Canonical Allele Identifier: CA1720489547

Gene: SEMA3C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.80902957_80902958delinsAG , CM000669.2:g.80902957_80902958delinsAG	GRCh38
NC_000007.13:g.80532273_80532274delinsAG , CM000669.1:g.80532273_80532274delinsAG	GRCh37
NC_000007.12:g.80370209_80370210delinsAG	NCBI36
NG_054744.1:g.24422_24423delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265361.8:c.103+13721_103+13722delinsCT MANE Select	ENSP00000265361.3:n.103+13721_103+13722delinsCT
ENST00000265361.7:c.103+13721_103+13722delinsCT	ENSP00000265361.3:n.103+13721_103+13722delinsCT
ENST00000411788.5:c.191+2871_191+2872delinsCT	ENSP00000395398.1:n.191+2871_191+2872delinsCT
ENST00000419255.6:c.103+13721_103+13722delinsCT	ENSP00000411193.2:n.103+13721_103+13722delinsCT
ENST00000427167.5:c.191+2871_191+2872delinsCT	ENSP00000399891.1:n.191+2871_191+2872delinsCT
ENST00000458729.5:c.103+13721_103+13722delinsCT	ENSP00000393825.1:n.103+13721_103+13722delinsCT
ENST00000487621.5:n.496+13721_496+13722delinsCT
NM_006379.3:c.103+13721_103+13722delinsCT	NP_006370.1:n.103+13721_103+13722delinsCT
XM_005250113.1:c.-72+2871_-72+2872delinsCT	XP_005250170.1:n.-72+2871_-72+2872delinsCT
NM_001350120.1:c.157+13721_157+13722delinsCT	NP_001337049.1:n.157+13721_157+13722delinsCT
NM_001350121.1:c.-72+2871_-72+2872delinsCT	NP_001337050.1:n.-72+2871_-72+2872delinsCT
NM_006379.4:c.103+13721_103+13722delinsCT	NP_006370.1:n.103+13721_103+13722delinsCT
NM_006379.5:c.103+13721_103+13722delinsCT MANE Select	NP_006370.1:n.103+13721_103+13722delinsCT
NM_001350120.2:c.157+13721_157+13722delinsCT	NP_001337049.1:n.157+13721_157+13722delinsCT
NM_001350121.2:c.-72+2871_-72+2872delinsCT	NP_001337050.1:n.-72+2871_-72+2872delinsCT